Immunofluorescence analysis of V5 tag was done on HEK-293 cells transiently overexpressing V5-His -LacZ. The cells were fixed with 4% paraformaldehyde for 15 minutes, permeabilized with 0.25% Triton™ X-100 for 10 minutes, and blocked with 5% BSA for 1 hour at room temperature. The cells were labeled with V5 Tag Mouse Monoclonal Antibody (377500) at a dilution of 1:500 in 1% BSA and incubated for 3 hours at room temperature and then labeled with Alexa Flour® 488 Rabbit Anti-Mouse IgG Secondary Antibody (A11059) at a dilution of 1:400 for 30 minutes at room temperature (Panel a: green). Nuclei (Panel b: blue) were stained with SlowFade® Gold Antifade Mountant with DAPI (S36938). F-actin (Panel c: red) was stained with Alexa Fluor® 594 Phalloidin (A12381). Panel d is a merged image showing cytoplasmic localization. Panel e is untransfected HEK-293 cells. The images were captured using a Nikon microscope at 20X magnification.
|Tested species reactivity||Mouse|
|Published species reactivity||Not Applicable|
|Host / Isotype||Rabbit / IgG|
|Immunogen||Gamma Immunoglobins Heavy and Light chains|
|Conjugate||Alexa Fluor® 488|
|Storage buffer||PBS, pH 7.5|
|Contains||5mM sodium azide|
|Storage Conditions||4° C, store in dark|
|Cross Adsorption||Against human serum prior to conjugation|
|Antibody Form||Whole Antibody|
|Tested Applications||Dilution *|
|Flow Cytometry (Flow)||1:100-1:500|
|Immunocytochemistry (ICC)||1-10 µg/mL|
|Immunofluorescence (IF)||1-10 µg/mL|
|Immunohistochemistry (IHC)||1-10 µg/ml|
* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.
To minimize cross-reactivity, these rabbit anti-mouse IgG (H+L) whole secondary antibodies have been affinity purified and cross-adsorbed against human serum prior to conjugation. Cross-adsorption or pre-adsorption is a purification step to increase specificity of the antibody resulting in higher sensitivity and less background staining. The secondary antibody solution is passed through a column matrix containing immobilized serum proteins from potentially cross-reactive species. Only the nonspecific-binding secondary antibodies are captured in the column, and the highly specific secondaries flow through. The benefits of this extra step are apparent in multiplexing/multicolor-staining experiments (e.g., flow cytometry) where there is potential cross-reactivity with other primary antibodies or in tissue/cell fluorescent staining experiments where there are may be the presence of endogenous immunoglobulins.
Alexa Fluor dyes are among the most trusted fluorescent dyes available today. Invitrogen™ Alexa Fluor 488 dye is a bright, green-fluorescent dye with excitation ideally suited to the 488 nm laser line. For stable signal generation in imaging and flow cytometry, Alexa Fluor 488 dye is pH-insensitive over a wide molar range. Probes with high fluorescence quantum yield and high photostability allow detection of low-abundance biological structures with great sensitivity. Alexa Fluor 488 dye molecules can be attached to proteins at high molar ratios without significant self-quenching, enabling brighter conjugates and more sensitive detection. The degree of labeling for each conjugate is typically 2-8 fluorophore molecules per IgG molecule; the exact degree of labeling is indicated on the certificate of analysis for each product lot.
Using conjugate solutions: Centrifuge the protein conjugate solution briefly in a microcentrifuge before use; add only the supernatant to the experiment. This step will help eliminate any protein aggregates that may have formed during storage, thereby reducing nonspecific background staining. Because staining protocols vary with application, the appropriate dilution of antibody should be determined empirically. For the fluorophore-labeled antibodies a final concentration of 1-10 µg/mL should be satisfactory for most immunohistochemistry and 1:100-1:500 for flow cytometry applications.
We offer an extensive line of Invitrogen™ secondary antibody conjugates with well-characterized specificity and labeled with a wide selection of premium fluorescent dyes, including Invitrogen™ Alexa Fluor™ fluorescent dyes. Fluorescent secondary antibody conjugates are useful in the detection, sorting, or purification of its specified target and ideal for fluorescence microscopy and confocal laser scanning microscopy, flow cytometry, and fluorescent western detection. The breadth of fluorescent markers we offer allows our reagents to be tailored to almost any fluorescent detection system.
Secondary antibodies may be provided in three formats: whole IgG, divalent F(ab')2 fragments, and monovalent Fab fragments. Because of the high degree of conservation in the structure of many immunoglobulin domains, most class-specific secondary antibodies must be affinity-purified and cross-adsorbed to achieve minimal cross-reaction with other immunoglobulins.
Our secondary antibody conjugates are most commonly prepared by immunizing the host animal with a pooled population of immunoglobulins from the target species and can be further purified and modified (e.g., immunoaffinity chromatography, antibody fragmentation, label conjugation, etc.) to generate highly specific reagents. In the first round of purification, whole immunoglobulins binding to the immunizing antibody are recovered and mainly consist of the ~150-kDa IgG class. Further purification, for example, with Protein A or G, removes all unwanted immunoglobulin classes except the affinity-purified antibodies that react with the target-specific immunoglobulin heavy and/or light chains.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
|Not Applicable||2 mg/ml||
DUX4-induced constitutive DNA damage and oxidative stress contribute to aberrant differentiation of myoblasts from FSHD patients.
A-11059 was used in flow cytometry to suggest that DNA damage induction is a novel function of DUX4 that affects myogenic differentiation of facioscapulohumeral dystrophy myoblasts
|Dmitriev P,Bou Saada Y,Dib C,Ansseau E,Barat A,Hamade A,Dessen P,Robert T,Lazar V,Louzada RA,Dupuy C,Zakharova V,Carnac G,Lipinski M,Vassetzky YS||Free radical biology and medicine (99:244)||2016|
|Not Applicable||Not Cited||
STAM2, a member of the endosome-associated complex ESCRT-0 is highly expressed in neurons.
A-11059 was used in immunohistochemistry - frozen section to study STAM2 in the nervous system
|Kapuralin K,¿urlin M,Mitre¿i¿ D,Kosi N,Schwarzer C,Glavan G,Gajovi¿ S||Molecular and cellular neurosciences (67:104)||2015|
|Not Applicable||Not Cited||
EGF regulates tyrosine phosphorylation and membrane-translocation of the scaffold protein Tks5.
A-11059 was used in immunocytochemistry to discuss the role of Tks4 in EGF signaling
|Fekete A,B¿gel G,Pesti S,Péterfi Z,Geiszt M,Buday L||Journal of molecular signaling (8:null)||2014|
|Not Applicable||Not Cited||Invasive fungal infection and impaired neutrophil killing in human CARD9 deficiency.||Drewniak A,Gazendam RP,Tool AT,van Houdt M,Jansen MH,van Hamme JL,van Leeuwen EM,Roos D,Scalais E,de Beaufort C,Janssen H,van den Berg TK,Kuijpers TW||Blood (121:2385)||2013|
|Not Applicable||Not Cited||Bleaching/blinking assisted localization microscopy for superresolution imaging using standard fluorescent molecules.||Burnette DT,Sengupta P,Dai Y,Lippincott-Schwartz J,Kachar B||Proceedings of the National Academy of Sciences of the United States of America (108:21081)||2011|
|Not Applicable||Not Cited||Reducing the multidimensionality of high-content screening into versatile powerful descriptors.||Gorenstein J,Zack B,Marszalek JR,Bagchi A,Subramaniam S,Carroll P,Elbi C||BioTechniques (49:663)||2010|
|Not Applicable||Not Cited||Functional protein delivery into neurons using polymeric nanoparticles.||Hasadsri L,Kreuter J,Hattori H,Iwasaki T,George JM||The Journal of biological chemistry (284:6972)||2009|
|Not Applicable||Not Cited||Stress induced morphological microglial activation in the rodent brain: involvement of interleukin-18.||Sugama S,Fujita M,Hashimoto M,Conti B||Neuroscience (146:1388)||2007|
|Not Applicable||Not Cited||Defined substrates for human embryonic stem cell growth identified from surface arrays.||Derda R,Li L,Orner BP,Lewis RL,Thomson JA,Kiessling LL||ACS chemical biology (2:347)||2007|
|Not Applicable||Not Cited||High-throughput tool for discovery of bone regulating factors.||Sharma P,Solomon KR,Hauschka PV||BioTechniques (41:539)||2006|
|Not Applicable||Not Cited||Systems biology in cancer research: genomics to cellomics.||Stilwell JL,Guan Y,Neve RM,Gray JW||Methods in molecular biology (Clifton, N.J.) (356:353)||2006|
|Not Applicable||Not Cited||Intracellular phospho-protein staining techniques for flow cytometry: monitoring single cell signaling events.||Krutzik PO,Nolan GP||Cytometry. Part A : the journal of the International Society for Analytical Cytology (55:61)||2003|
|Not Applicable||Not Cited||Estrogens inhibit l-glutamate uptake activity of astrocytes via membrane estrogen receptor alpha.||Sato K,Matsuki N,Ohno Y,Nakazawa K||Journal of neurochemistry (86:1498)||2003|
|Not Applicable||Not Cited||Differential expression of heparan sulfate domains in rat spleen.||ten Dam GB,Hafmans T,Veerkamp JH,van Kuppevelt TH||The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society (51:727)||2003|
|Not Applicable||Not Cited||Ribonucleoprotein-dependent localization of the yeast class V myosin Myo4p.||Kruse C,Jaedicke A,Beaudouin J,Bohl F,Ferring D,Guttler T,Ellenberg J,Jansen RP||The Journal of cell biology (159:971)||2002|
|Not Applicable||Not Cited||A new blocking method for application of murine monoclonal antibody to mouse tissue sections.||Lu QL,Partridge TA||The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society (46:977)||1998|